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联系我们
+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
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Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Chiral Compounds
Deuterated
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Indoles and Oxindoles
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联系我们
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产品名字索引 A
按首字母搜索
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产品名字索引 A
Alantolactone
(Catalog# : 161227107, Cas# :
546-43-0
)
Alantolactone, a naturally occurring eudesmane-type sesquiterpene lactone (SL), could
AS101
(Catalog# : 161227106, Cas# :
106566-58-9
)
AS101, a potent in vitro and in vivo immunomodulator, is a novel inhibitor of IL-1bet
ACP-196
(Catalog# : 16122783, Cas# :
1420477-60-6
)
Acalabrutinib is a selective second-generation Brutons tyrosine kinase (BTK) inhibito
APS-2-79
(Catalog# : 16122775, Cas# :
2002381-31-7
)
APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antago
Aprotinin
(Catalog# : 16122761, Cas# :
9087-70-1
)
Aprotinin is a small protein serine protease inhibitor, used to reduce perioperative
A-366
(Catalog# : 16122743, Cas# :
1527503-11-2
)
A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor wi
AZD0156
(Catalog# : 16122713, Cas# :
1821428-35-6
)
AZD0156 is a potent and selective inhibitors of ATM kinase, with potential chemo-/rad
APTSTAT3-9R
(Catalog# : 16122704)
APTSTAT3-9R is a specific STAT3-binding peptide with addition of a cell-penetrating m
AGN 205728
(Catalog# : 6111520, Cas# :
859498-05-8
)
AGN 205728 is a potent and selective RAR antagonist with Ki/IC95 values of 3 nM/ 0.6
AGN 205327
(Catalog# : 6111519)
AGN 205327 is a potent synthetic RARs agonist with EC50 of 3766/734/32 nM for RAR// r
AGN 195183
(Catalog# : 6111517, Cas# :
367273-07-2
)
AGN 195183 is a potent and selective agonist of RAR(Kd=3 nM) with improved binding se
AGN 194310
(Catalog# : 6111516, Cas# :
229961-45-9
)
AGN 194310(VTP-194310) is a potent and selective pan-RARs agonist with Kd values of 3
Acetazolamide D3
(Catalog# : 6111513, Cas# :
1189904-01-5
)
Acetazolamide D3 is deuterium labeled Acetazolamide, which is a potent carbonic anhyd
APS-2-79
(Catalog# : 6111501, Cas# :
2002381-25-9
)
APS-2-79 is an antagonist of MEK phosphorylation by RAF through direct binding of the
(+)-Apogossypol
(Catalog# : 61125, Cas# :
66389-74-0
)
(+)-Apogossypol(Apogossypol; NSC736630) is a potent inhibitor of Bcl-2 family protein
A-836339
(Catalog# : 6111107, Cas# :
959746-77-1
)
A-836339 is a cannabinoid CB2 receptor-selective agonist; exhibits high potencies at
AB-MECA
(Catalog# : 6111105, Cas# :
152918-26-8
)
AB-MECA is a high affinity A3 adenosine receptor agonist, has high affinity for recom
Amitifadine hydrochloride
(Catalog# : 6111104, Cas# :
410074-74-7
)
Amitifadine hydrochloride is a triple reuptake inhibitor (TRI) or serotonin-norepinep
ATI-2341
(Catalog# : 6111101, Cas# :
1337878-62-2
)
ATI-2341, pepducin targeting the C-X-C chemokine receptor type 4 (CXCR4), is an allos
Auristatin F
(Catalog# : 6111022, Cas# :
163768-50-1
)
Auristatin F is a cytotoxic tubulin modifier with potent and selective antitumor acti
Auristatin E
(Catalog# : 6111021, Cas# :
160800-57-7
)
Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor acti
ABT-639
(Catalog# : 6111011, Cas# :
1235560-28-7
)
ABT-639 is a novel, peripherally acting, selective T-type Ca2+ channel blocker. ABT-6
3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile
(Catalog# : 6111001, Cas# :
21230-50-2
)
3-aMino-1-Methyl-1H-pyrazole-4-carbonitrile 21230-50-2
360A
(Catalog# : 611935, Cas# :
794458-56-3
)
360A is a strong affinity and selectivity inhibitor of G-quadruplex structures.
AT7519 trifluoroacetate
(Catalog# : 611916, Cas# :
1431697-85-6
)
AT7519 trifluoroacetate is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of
Ampkinone
(Catalog# : 611810, Cas# :
1233082-79-5
)
Ampkinone is a small molecule activator of AMPK; stimulate functional activation of A
AT7867 dihydrochloride
(Catalog# : 611806, Cas# :
1431697-86-7
)
AT7867 Hcl is a potent ATP-competitive inhibitor of Akt1/2/3 and p70S6K/PKA with IC50
ARQ-092
(Catalog# : 611805, Cas# :
1313881-70-7
)
ARQ-092 is an Akt inhibitor extracted from patent US/20150299195A1, compound A.
Akt1 and Akt2-IN-1
(Catalog# : 611804, Cas# :
893422-47-4
)
Akt1 and Akt2-IN-1 is an allosteric inhibitor of Akt1 (IC50 = 3.5 nM) and Akt2 (IC50
AKT inhibitor
(Catalog# : 611803, Cas# :
1004990-28-6
)
AKT inhibitor is a broadly selective, potent, ATP-competitive Akt inhibitor, displays
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产品分类
信号通路
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
----
Methionine Adenosyltransferase (MAT)
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
----
Proton Pump
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
----
CGRP-Receptor
----
TRP-Channel
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
-- Nuclear Receptor
----
Androgen Receptor(AR)
抑制剂/受体激动剂
中间体
分子砌块
--
Aldehydes
--
Amines
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
新产品
天然化合物
最新产品
Kartogenin ( KGN )
(Catalog# : 52215, Cas# :
4727-31-5
)
Kartogenin(KGN)是一种合成小分子,通过激活smad-4/5通路刺激软骨细
Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602, Cas# :
218791-21-0
)
Imisopasem manganese ( M40403; GC4403 ) 是一种稳定的非肽类 MnSOD 类似物,
Apecotrep (BI 764198)
(Catalog# : 26A048, Cas# :
2311863-36-0
)
Apecotrep(BI 764198)是一种潜在的同类首创、口服、选择性的TRPC6抑
Pantothenate kinase-IN-2
(Catalog# : 26A038, Cas# :
902614-04-4
)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,
BH-30643
(Catalog# : 26A047, Cas# :
3062177-59-4
)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制
Gridegalutamide
(Catalog# : 26A044, Cas# :
2446929-86-6
)
格列德加鲁胺是一种具有口服生物利用度的雄激素受体(AR)降解
BMS-986365 (别名: CC-94676 )
(Catalog# : 25138, Cas# :
2446928-30-7
)
BMS-986365,也称为 CC-94676,是一种口服生物可利用的雄激素受体 (A
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
VAS3947
(Catalog# : 20302, Cas# :
869853-70-3
)
VAS3947是一种低微摩尔浓度的NADPH氧化酶活性的选择性抑制剂,既不